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dc.contributor.authorSanthasiri Orrapinen_US
dc.contributor.authorSittiruk Roytrakulen_US
dc.contributor.authorNarumon Phaonakropen_US
dc.contributor.authorSiriwan Thaisakunen_US
dc.contributor.authorKhajornsak Tragoolpuaen_US
dc.contributor.authorAmornrat Intorasooten_US
dc.contributor.authorSuzanne McGillen_US
dc.contributor.authorRichard Burchmoreen_US
dc.contributor.authorSorasak Intorasooten_US
dc.date.accessioned2022-10-16T07:00:24Z-
dc.date.available2022-10-16T07:00:24Z-
dc.date.issued2021-11-01en_US
dc.identifier.issn14203049en_US
dc.identifier.other2-s2.0-85119918263en_US
dc.identifier.other10.3390/molecules26227011en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85119918263&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/75512-
dc.description.abstractThe occurrence of Cryptococcus neoformans, the human fungal pathogen that primarily infects immunocompromised individuals, has been progressing at an alarming rate. The increased incidence of infection of C. neoformans with antifungal drugs resistance has become a global concern. Potential antifungal agents with extremely low toxicity are urgently needed. Herein, the biological activities of recombinant javanicin (r-javanicin) against C. neoformans were evaluated. A time-killing assay was performed and both concentration-and time-dependent antifungal activity of r-javanicin were indicated. The inhibitory effect of the peptide was initially observed at 4 h post-treatment and ultimately eradicated within 36 to 48 h. Fungal outer surface alteration was characterized by the scanning electron microscope (SEM) whereas a negligible change with slight shrinkage of external morphology was observed in r-javanicin treated cells. Confocal laser scanning microscopic analysis implied that the target(s) of r-javanicin is conceivably resided in the cell thereby allowing the peptide to penetrate across the membrane and accumulate throughout the fungal body. Finally, cryptococcal cells coped with r-javanicin were preliminarily investigated using label-free mass spectrometry-based proteomics. Combined with microscopic and proteomics analysis, it was clearly elucidated the peptide localized in the intracellular compartment where carbohydrate metabolism and energy production associated with glycolysis pathway and mitochondrial respiration, respectively, were principally interfered. Overall, r-javanicin would be an alternative candidate for further development of antifungal agents.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleFungicidal activity of recombinant javanicin against cryptococcus neoformans is associated with intracellular target(S) involved in carbohydrate and energy metabolic processesen_US
dc.typeJournalen_US
article.title.sourcetitleMoleculesen_US
article.volume26en_US
article.stream.affiliationsThailand National Center for Genetic Engineering and Biotechnologyen_US
article.stream.affiliationsCollege of Medical, Veterinary & Life Sciencesen_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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